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Ethanol → 2-Fluoro-4'-aminobenzophenone

HRID 865254
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 865254
[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.[NH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(O)C>O>[NH2:11][C:12]1[CH:17]=[CH:16][C:15]([C:4]([C:3]2[CH:7]=[CH:8][CH:9]=[CH:10][C:2]=2[F:1])=[O:6])=[CH:14][CH:13]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 702EthanolHCID 6115AnilineHCID 99352-Fluorobenzoic acid

Produkt 1

HCID 105128532-Fluoro-4'-aminobenzophenoneAusbeute 253,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

To stirred 90° C. polyphosphoric acid (200 g) was added 14.29 g (10.2 mmol) of 2-fluorobenzoic acid and aniline (9.32 g 10.0 mmol) and the bath temperature raised to 180°-190° C. and held there for 1 hour. A solution was obtained at about 140° C. The heating bath was removed and the stirred mixture (sublimate above the solution) was treated cautiously with 80 mL of water. The mixture was stirred at 140°-155° C. for 1 hour, the heating bath removed, 66 mL of 3N HCl added, the mixture poured into 1L of water and filtered through a pad of Celite. The liltrate was basilled with 15% sodium hydroxide and the solid which formed on stirring was collected. The Celite pad was washed well with methylene chloride, the methylene chloride removed and the residue was combined with the solid obtained from basification of the aqueous phase. The combined material was dissolved in refluxing ethanol (175 mL), and treated hot with 125 mL of water. The brown solid obtaing on cooling was additionally recrystallized twice from ethyl acetate - hexane. Final purification by flash column chromatography (methylene chloride) yielded the aniline as a white solid (5.45 g, 25%); mp 128°-130° C. 1H-NMR (250 MHz, d6-DMSO): 6.32 (s, 2H, NH2) 6.60 (dd, 2H, J=8.6, 1.5 Hz, aromatic) 7.28-7.35 (m, 2H, aromatic) 7.40-7.60 (m, 4H, aromatic). MS (CI, CH4): 216 (M+1).

Aufarbeitung

  1. temperaturethe bath temperature raised to 180°-190° C.
  2. customA solution was obtained at about 140° C
  3. customThe heating bath was removed
  4. additionthe stirred mixture (sublimate above the solution) was treated cautiously with 80 mL of water
  5. customthe heating bath removed
  6. addition66 mL of 3N HCl added
  7. additionthe mixture poured into 1L of water
  8. filtrationfiltered through a pad of Celite
  9. customthe solid which formed
  10. stirringon stirring
  11. customwas collected
  12. washThe Celite pad was washed well with methylene chloride
  13. customthe methylene chloride removed
  14. customobtained from basification of the aqueous phase
  15. dissolutionThe combined material was dissolved
  16. temperatureThe brown solid obtaing on cooling
  17. customwas additionally recrystallized twice from ethyl acetate - hexane
  18. customFinal purification by flash column chromatography (methylene chloride)

Quellen und Nachweise

ORD-Eintrag
ord-7dc29f96500647ec802d9cc4d3c408b8
Quelldatensatz
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05565477

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